A single aspartate mutation in the conserved catalytic site of Rev3L generates a hypomorphic phenotype in vivo and in vitro

Rémi Fritzen, Frédéric Delbos, Annie De Smet, Benoît Palancade, Christine E Canman, Said Aoufouchi, Jean-Claude Weill, Claude-Agnès Reynaud, Sébastien Storck

Research output: Contribution to journal › Article › peer-review

7 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology